Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2015000500477&lng=en&nrm=iso&tlng=en http://hdl.handle.net/11449/129676 |
Resumo: | The transgenic application of green fluorescent protein (GFP) as fetal cell marker on cattle cloned placenta could provide an exclusive model for studying the morphologic and immunologic maternal-fetal interactions, providing information about its mapping, distinguishing the fetal from maternal cells. This model will have direct application, mainly because these animals present problems during its development. With this model's support, we intend to verify the substances transport between mother and fetus during endocytosis, through the immunolocalization of protein named caveolae. For these, we used 06 cloned bovine and 30 cattle samples of artificial insemination (AI) with 90 days of pregnancy, which had been their development interrupted by humanitarian slaughter of the recipient and recovery of the pregnant uterus. We collected the placentome and the chorion. A part of the samples was cut and fixed, by immersion, on a solution containing 4% of parafomaldehyde or 10% of formaldehyde on a sodium phosphate buffer (PBS), at 0,1 M pH 7.4, Zamboni solution (4% of paraformaldehyde, 15% of picric acid, on sodium phosphate buffer 0,1 M pH 7.4), metacarn (60% of metanol, 30% of chloroform, and 10% glacial acetic acid), for morphologic and immunohistochemistry verification for caveolinas proteins -1 and -2 (CAV -1 and CAV-2). The caveolins -1 were found in fetal and maternal villi, but its strongest staining was observed in the endometrial stroma. The caveolins -2 had positive staining in trophoblast and chorioallantoic membrane, and specifically in giant trophoblastic binucleated cell. Therefore the results were compared between cloned cattle and from AI or natural mating, for assisting on detection of the reason of many placental alterations, embryonic losses, spontaneous abortion, post-natal mortality and large offspring syndrome on laboratory-manipulated animals. The result suggests that the proteins caveolins -1 and -2 (CAV-1 and CAV-2) are part of the caveolae composition and important structures related to the molecule transfer to the fetus, nourish it through endocytosis and pinocytosis. |
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Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicosCaracterization of caveolin -1 and -2 proteins in cloned and transgenic placenta of cattleCaveolin-1 and-2 proteinsCaveolaePlacentationImmunolocalizationCattleProteínas caveolinas -1 e -2Placenta de conceptos bovinos clonadosTransgênicosCavéolaCaveolinaPlacentaçãoImunolocalizaçãoThe transgenic application of green fluorescent protein (GFP) as fetal cell marker on cattle cloned placenta could provide an exclusive model for studying the morphologic and immunologic maternal-fetal interactions, providing information about its mapping, distinguishing the fetal from maternal cells. This model will have direct application, mainly because these animals present problems during its development. With this model's support, we intend to verify the substances transport between mother and fetus during endocytosis, through the immunolocalization of protein named caveolae. For these, we used 06 cloned bovine and 30 cattle samples of artificial insemination (AI) with 90 days of pregnancy, which had been their development interrupted by humanitarian slaughter of the recipient and recovery of the pregnant uterus. We collected the placentome and the chorion. A part of the samples was cut and fixed, by immersion, on a solution containing 4% of parafomaldehyde or 10% of formaldehyde on a sodium phosphate buffer (PBS), at 0,1 M pH 7.4, Zamboni solution (4% of paraformaldehyde, 15% of picric acid, on sodium phosphate buffer 0,1 M pH 7.4), metacarn (60% of metanol, 30% of chloroform, and 10% glacial acetic acid), for morphologic and immunohistochemistry verification for caveolinas proteins -1 and -2 (CAV -1 and CAV-2). The caveolins -1 were found in fetal and maternal villi, but its strongest staining was observed in the endometrial stroma. The caveolins -2 had positive staining in trophoblast and chorioallantoic membrane, and specifically in giant trophoblastic binucleated cell. Therefore the results were compared between cloned cattle and from AI or natural mating, for assisting on detection of the reason of many placental alterations, embryonic losses, spontaneous abortion, post-natal mortality and large offspring syndrome on laboratory-manipulated animals. The result suggests that the proteins caveolins -1 and -2 (CAV-1 and CAV-2) are part of the caveolae composition and important structures related to the molecule transfer to the fetus, nourish it through endocytosis and pinocytosis.A utilização da transgenia com a proteína fluorescente verde (GFP) como marcador de células de origem fetal nas placentas de clones bovinos servirá de modelo inédito para estudo morfofisiológico e imunológico da interação materno-fetal, visto que possibilitará o seu mapeamento, diferenciando as células fetais das maternas. Tal modelo terá aplicação direta, principalmente porque estes são animais que apresentam problemas em relação ao seu desenvolvimento. Com o auxílio deste modelo, pretende-se verificar o transporte de substâncias entre a mãe e o feto via endocitose, pela imunolocalização das proteínas chamadas de caveolinas. Para tanto foram utilizados 06 bovinos clonados e 30 bovinos de inseminação artificial (IA) com idade até 90 dias de gestação, os quais tiveram seu desenvolvimento interrompido mediante abate humanitário das receptoras e ovariosalpingohisterectomia, com posterior recuperação do útero gestante. Foram coletados os placentônios e o cório. Uma parte das amostras foi recortada e fixada, por imersão, em solução de parafolmaldeído a 4% ou formoldeído a 10% em tampão fosfato de sódio (PBS) a 0,1M pH 7.4, solução de Zamboni (4% de paraformoldeído, 15% de ácido pícrico, em tampão fosfato de sódio a 0,1M pH 7.4), metacarn (60% de metanol, 30% de clorofórmio, e 10% de ácido acético glacial), para verificação da morfologia e realização de imuno-histoquímica para as proteínas caveolinas -1 e -2 (CAV -1 e CAV-2). As caveolinas -1 foram localizadas nos vilos fetais e maternos, mas sua marcação mais forte foi observada no estroma endometrial. As caveolinas -2 tiveram marcação positiva no trofoblasto e membrana córioalantoide, e, especificamente em célula trofoblástica gigante binucleada. Sendo assim, os resultados mostram que a proteína CAV-1 teve uma maior expressão em relação à proteína CAV-2 e que as proteínas CAV-1 e -2 são parte da composição das cavéolas, sendo estruturas importantes e relacionadas com a transferência de moléculas para o feto, realizando a nutrição do mesmo mediante endocitose e pinocitose.Univ Estadual Paulista Julio de Mesquita Filho Un, Lab Morfofisiol Placenta &Embriao, BR-17900000 Dracena, SP, BrazilMichigan State Univ, Dept Anim Sci, E Lansing, MI 48824 USAUniv Sao Paulo, Fac Zootecnia &Engn Alimentos, Lab Morfofisiol Mol Desenvolvimento, BR-13635900 Pirassununga, SP, BrazilUniv Estadual Paulista Julio de Mesquita Filho, Lab Morfofisiol Placenta & Embriao, BR-17900000 Dracena, SP, BrazilRevista Pesquisa Veterinaria BrasileiraUniversidade Estadual Paulista (Unesp)Michigan State UnivUniversidade de São Paulo (USP)Peres, Kenya C. [UNESP]Trinca, Vitor [UNESP]Oliveira, Fernanda P. [UNESP]Oliveira, Lilian J.Bressan, Fabiana F.Pimentel, Jose R. V.Meirelles, Flavio V.Pereira, Flávia Thomaz Verechia [UNESP]2015-10-22T06:28:22Z2015-10-22T06:28:22Z2015-05-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article477-485application/pdfhttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2015000500477&lng=en&nrm=iso&tlng=enPesquisa Veterinaria Brasileira, v. 35, n. 5, p. 477-485, 2015.0100-736Xhttp://hdl.handle.net/11449/12967610.1590/S0100-736X-2015000500016S0100-736X2015000500477WOS:000357746000016S0100-736X2015000500477.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporPesquisa Veterinaria Brasileira0.385info:eu-repo/semantics/openAccess2024-05-07T13:59:32Zoai:repositorio.unesp.br:11449/129676Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T13:58:46.030144Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos Caracterization of caveolin -1 and -2 proteins in cloned and transgenic placenta of cattle |
title |
Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos |
spellingShingle |
Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos Peres, Kenya C. [UNESP] Caveolin-1 and-2 proteins Caveolae Placentation Immunolocalization Cattle Proteínas caveolinas -1 e -2 Placenta de conceptos bovinos clonados Transgênicos Cavéola Caveolina Placentação Imunolocalização |
title_short |
Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos |
title_full |
Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos |
title_fullStr |
Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos |
title_full_unstemmed |
Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos |
title_sort |
Caracterização das proteínas caveolinas -1 e -2 na placenta de conceptos bovinos clonados transgênicos |
author |
Peres, Kenya C. [UNESP] |
author_facet |
Peres, Kenya C. [UNESP] Trinca, Vitor [UNESP] Oliveira, Fernanda P. [UNESP] Oliveira, Lilian J. Bressan, Fabiana F. Pimentel, Jose R. V. Meirelles, Flavio V. Pereira, Flávia Thomaz Verechia [UNESP] |
author_role |
author |
author2 |
Trinca, Vitor [UNESP] Oliveira, Fernanda P. [UNESP] Oliveira, Lilian J. Bressan, Fabiana F. Pimentel, Jose R. V. Meirelles, Flavio V. Pereira, Flávia Thomaz Verechia [UNESP] |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Michigan State Univ Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Peres, Kenya C. [UNESP] Trinca, Vitor [UNESP] Oliveira, Fernanda P. [UNESP] Oliveira, Lilian J. Bressan, Fabiana F. Pimentel, Jose R. V. Meirelles, Flavio V. Pereira, Flávia Thomaz Verechia [UNESP] |
dc.subject.por.fl_str_mv |
Caveolin-1 and-2 proteins Caveolae Placentation Immunolocalization Cattle Proteínas caveolinas -1 e -2 Placenta de conceptos bovinos clonados Transgênicos Cavéola Caveolina Placentação Imunolocalização |
topic |
Caveolin-1 and-2 proteins Caveolae Placentation Immunolocalization Cattle Proteínas caveolinas -1 e -2 Placenta de conceptos bovinos clonados Transgênicos Cavéola Caveolina Placentação Imunolocalização |
description |
The transgenic application of green fluorescent protein (GFP) as fetal cell marker on cattle cloned placenta could provide an exclusive model for studying the morphologic and immunologic maternal-fetal interactions, providing information about its mapping, distinguishing the fetal from maternal cells. This model will have direct application, mainly because these animals present problems during its development. With this model's support, we intend to verify the substances transport between mother and fetus during endocytosis, through the immunolocalization of protein named caveolae. For these, we used 06 cloned bovine and 30 cattle samples of artificial insemination (AI) with 90 days of pregnancy, which had been their development interrupted by humanitarian slaughter of the recipient and recovery of the pregnant uterus. We collected the placentome and the chorion. A part of the samples was cut and fixed, by immersion, on a solution containing 4% of parafomaldehyde or 10% of formaldehyde on a sodium phosphate buffer (PBS), at 0,1 M pH 7.4, Zamboni solution (4% of paraformaldehyde, 15% of picric acid, on sodium phosphate buffer 0,1 M pH 7.4), metacarn (60% of metanol, 30% of chloroform, and 10% glacial acetic acid), for morphologic and immunohistochemistry verification for caveolinas proteins -1 and -2 (CAV -1 and CAV-2). The caveolins -1 were found in fetal and maternal villi, but its strongest staining was observed in the endometrial stroma. The caveolins -2 had positive staining in trophoblast and chorioallantoic membrane, and specifically in giant trophoblastic binucleated cell. Therefore the results were compared between cloned cattle and from AI or natural mating, for assisting on detection of the reason of many placental alterations, embryonic losses, spontaneous abortion, post-natal mortality and large offspring syndrome on laboratory-manipulated animals. The result suggests that the proteins caveolins -1 and -2 (CAV-1 and CAV-2) are part of the caveolae composition and important structures related to the molecule transfer to the fetus, nourish it through endocytosis and pinocytosis. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-10-22T06:28:22Z 2015-10-22T06:28:22Z 2015-05-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2015000500477&lng=en&nrm=iso&tlng=en Pesquisa Veterinaria Brasileira, v. 35, n. 5, p. 477-485, 2015. 0100-736X http://hdl.handle.net/11449/129676 10.1590/S0100-736X-2015000500016 S0100-736X2015000500477 WOS:000357746000016 S0100-736X2015000500477.pdf |
url |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-736X2015000500477&lng=en&nrm=iso&tlng=en http://hdl.handle.net/11449/129676 |
identifier_str_mv |
Pesquisa Veterinaria Brasileira, v. 35, n. 5, p. 477-485, 2015. 0100-736X 10.1590/S0100-736X-2015000500016 S0100-736X2015000500477 WOS:000357746000016 S0100-736X2015000500477.pdf |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
Pesquisa Veterinaria Brasileira 0.385 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
477-485 application/pdf |
dc.publisher.none.fl_str_mv |
Revista Pesquisa Veterinaria Brasileira |
publisher.none.fl_str_mv |
Revista Pesquisa Veterinaria Brasileira |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
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1808128218128973824 |